Diazepam Guide, Meaning , Facts, Information and Description
Diazepam | |
| 7-chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepin-2-one | |
| Empiric formula | C16H13ClN2O |
| Molecular weight | 284.7 |
| Bioavailability | ? |
| Metabolism | Liver |
| Elimination half life | biphasic 1-2d/2-5d |
| Excretion | Urine |
| ATC code | N05BA01 |
| Pregnancy category | D (USA) C (Aus) |
| Table of contents |
|
2 Pharmacokinetics 3 Side effects |
Mode of action
Diazepam effects mainly the central nervous system. It binds in to specific benzodiazepine-receptors, which are part of the GABA-receptors. When diazepam binds to this receptor, it causes an increase in the inhibitory effects on GABA. The effect of diazepam does not last long, partly because it is fairly quickly redistributed into tissues and fat depots, and partly because of the adaptation of benzodiazepine receptors.
Pharmacokinetics
Diazepam can be administered orally, as an injection (i.v. and i.m.) or as suppositories. When taken orally, diazepam is rapidly absorbed. Absorption is much slower and erratic, when diazepam is given as as intramuscular injection. Diazepam is highly lipid-soluble, and therefore crosses the blood-brain barrier easily.
Diazepam is metabolised in the liver, and it has a biphasic half-life, the first phase half-life (t½α) is 24-48 hours, and its main active metabolites, desmethyldiazepam's, half-life is 2-5 days. Diazepam's other active metabolites include among others temazepam and oxazepam. Diazepam and its metabolites are excreted into the urine.